Phenotype and genotype in the myotonic disorders

Cardiac sodium channel structure and function.

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Scholarship in the medical faculty from the university perspective: retaining academic values.

Academic medicine : journal of the Association of American Medical Colleges·2000

Altered gene expression in steroid-treated denervated muscle.

Neurobiology of disease·1999

Dual tandem promoter elements containing CCAC-like motifs from the tetrodotoxin-resistant voltage-sensitive Na+ channel (rSkM2) gene can independently drive muscle-specific transcription in L6 cells.

Gene expression·1999

Interaction between the skeletal muscle type 1 Na+ channel promoter E-box and an upstream repressor element. Release of repression by myogenin.

The Journal of biological chemistry·1999

Ion channel mutations affecting muscle and brain.

Current opinion in neurology·1998

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LncRNASNHG12 regulates the development of diabetic nephropathy through miR-129-5p/IL6ST axis.

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Related Experiment Videos

Phenotype and genotype in the myotonic disorders

Related Concept Videos

Cardiac sodium channel structure and function.

Scholarship in the medical faculty from the university perspective: retaining academic values.

Altered gene expression in steroid-treated denervated muscle.

Dual tandem promoter elements containing CCAC-like motifs from the tetrodotoxin-resistant voltage-sensitive Na+ channel (rSkM2) gene can independently drive muscle-specific transcription in L6 cells.

Interaction between the skeletal muscle type 1 Na+ channel promoter E-box and an upstream repressor element. Release of repression by myogenin.

Ion channel mutations affecting muscle and brain.

"Abductor Sparing": A New Selective Involvement in ALS.

Enabling Functional Independence: A Scoping Review of Upper Extremity Assistive Devices for Adults With Progressive Neuromuscular Diseases.

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Quantitative Assessment of Tongue Atrophy in Amyotrophic Lateral Sclerosis Using Transoral Tongue Ultrasonography (TOTU): A Retrospective Single-Center Study.

Sensory Cortical Hyperexcitability in Amyotrophic Lateral Sclerosis Involves a Broad Hand Representation Within the Primary Somatosensory Cortex.

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Neuronal Cell-Specific sc-eQTL and Integrative eQTL-pQTL Mendelian Randomization Prioritize CKAP2 as a Candidate Gene for Major Depressive Disorder.

LncRNASNHG12 regulates the development of diabetic nephropathy through miR-129-5p/IL6ST axis.

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Phenotype and genotype in the myotonic disorders

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